rs35211496

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs35211496(C;T)

Make rs35211496(T;T)

Reference

GRCh38 38.1/141

Chromosome

18

Position

62354528

Gene

TNFRSF11A

is a	snp
is	mentioned by
dbSNP	rs35211496
dbSNP (classic)	rs35211496
ClinGen	rs35211496
ebi	rs35211496
HLI	rs35211496
Exac	rs35211496
Gnomad	rs35211496
Varsome	rs35211496
LitVar	rs35211496
Map	rs35211496
PheGenI	rs35211496
Biobank	rs35211496
1000 genomes	rs35211496
hgdp	rs35211496
ensembl	rs35211496
geneview	rs35211496
scholar	rs35211496
google	rs35211496
pharmgkb	rs35211496
gwascentral	rs35211496
openSNP	rs35211496
23andMe	rs35211496
SNPshot	rs35211496
SNPdbe	rs35211496
MSV3d	rs35211496
GWAS Ctlg	rs35211496

GMAF

0.08035

Max Magnitude

0

[PMID 20231205] Genetic Variations in Genes Encoding RANK, RANKL, and OPG in Rheumatoid Arthritis: A Case-Control Study

[PMID 20564239] Genetic variation in the TNFRSF11A gene encoding RANK is associated with susceptibility to Paget's disease of bone

[PMID 23369128] Genetic polymorphism of the OPG gene associated with breast cancer

[PMID 24921058] Receptor activator of nuclear factor kappa-B gene polymorphisms in Iranian periodontitis and peri-implantitis patients

ClinVar
Risk	rs35211496(T;T)
Alt	rs35211496(T;T)
Reference	Rs35211496(C;C)
Significance	Probable-non-pathogenic
Disease	Paget disease of bone Osteopetrosis not specified
Variation	info
Gene	TNFRSF11A
CLNDBN	Paget disease of bone Osteopetrosis not specified
Reversed	0
HGVS	NC_000018.9:g.60021761C>T
CLNSRC
CLNACC	RCV000269060.1, RCV000363657.1, RCV000454965.1,